- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
55 result(s) found for: Social stress.
Displaying page 1 of 3.
EudraCT Number: 2017-000298-35 | Sponsor Protocol Number: NL60593.028.17 | Start Date*: 2017-05-01 |
Sponsor Name:Tilburg University | ||
Full Title: Oxytocin, friendship and dealing with emotions | ||
Medical condition: There are no medical conditions or disease under investigation. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004177-83 | Sponsor Protocol Number: 37202 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting the oxytocin system in acute trauma: The effectiveness of intranasal oxytocin treatments and stimulation of social support on preventing trauma related psychopathology | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001878-29 | Sponsor Protocol Number: 35RC18_8852_PROPRADO | Start Date*: 2021-05-21 | |||||||||||
Sponsor Name:Rennes University Hospital | |||||||||||||
Full Title: The efficacy of traumatic memory modification using a memory reconsolidation procedure under propranolol among adolescents with post-traumatic stress disorder (PROPRADO) | |||||||||||||
Medical condition: post-traumatic stress disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006228-19 | Sponsor Protocol Number: PTF3 | Start Date*: 2012-03-21 | |||||||||||
Sponsor Name:Psykiatrisk Center Ballerup | |||||||||||||
Full Title: The treatment of traumatized refugees with Setraline versus Venlafaxine - a randomized trial. | |||||||||||||
Medical condition: Post traumatic stress disorder (PTSD) Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001288-58 | Sponsor Protocol Number: 40122 | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting oxytocin after trauma: The effects of intranasal oxytocin administration on emotional and motivational brain processes in PTSD | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005956-39 | Sponsor Protocol Number: RC31/18/0471 | Start Date*: 2021-04-06 | |||||||||||
Sponsor Name:CHU Toulouse | |||||||||||||
Full Title: Treatment of pediatric Post-traumatic Stress Disorder with memory reactivation under the influence of propranolol: A randomized placebo-controlled trial | |||||||||||||
Medical condition: Post-traumatic Stress Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004823-36 | Sponsor Protocol Number: AZ1-2004 | Start Date*: 2005-03-03 |
Sponsor Name:daacro - diagnostic assessment and clinical research organization | ||
Full Title: Effects of Alprazolam and Flupentixol on endocrine, autonomic and psychological parameters in the Trier Social Stress Test (TSST) | ||
Medical condition: 69 healthy male subjects, age 18-45 undergo a laboratory stress test (TSST) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000319-21 | Sponsor Protocol Number: ClonDO | Start Date*: 2021-12-20 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Treating Nightmares in Posttraumatic Stress Disorder with the α-adrenergic Agents Clonidine and Doxazosin: A Randomized-Controlled Feasibility Study (ClonDoTrial) | ||
Medical condition: Posttraumatic Stress Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003331-10 | Sponsor Protocol Number: HC03 | Start Date*: 2017-10-16 |
Sponsor Name:Leiden University | ||
Full Title: Acute effects of 40 mg cortisol on emotion and cognition. | ||
Medical condition: None. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001573-28 | Sponsor Protocol Number: Uni-Koeln-320 | Start Date*: 2007-11-26 |
Sponsor Name:Universität zu Köln | ||
Full Title: Prevent: Secondary Prevention of Schizophrenia. A randomized controlled trial. | ||
Medical condition: Persons at risk of being prodromally symptomatic of psychosis (PAR) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022686-10 | Sponsor Protocol Number: 578001.01.012 | Start Date*: 2011-06-08 |
Sponsor Name:Dr. W. Schwabe GmbH & Co. KG | ||
Full Title: Multi-centre, open-label clinical trial to evaluate the efficacy and safety of Rhodiola rosea extract WS® 1375 in Subjects with Burnout Symptoms | ||
Medical condition: Burnout symptoms like exhaustion, fatigue, mild anxiety, mood disturbances | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014049-10 | Sponsor Protocol Number: HP0749GE201 | Start Date*: 2009-11-27 | |||||||||||
Sponsor Name:Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: Exploratory study of besipirdine efficacy and safety in male patients with persistent stress urinary incontinence after radical prostatectomy | |||||||||||||
Medical condition: Persistant stress urinary incontinence further to radical prostatectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002436-82 | Sponsor Protocol Number: EC11-441 | Start Date*: 2012-12-13 |
Sponsor Name:Isabel Pinilla Lozano | ||
Full Title: Melatonin effects on visual and sleep patterns anomalies in subjects diagnosed with Retinitis Pigmentosa | ||
Medical condition: To evaluate the sleep quality in patients with Retinitis Pigmentosa | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001965-36 | Sponsor Protocol Number: FAAHIPTSD | Start Date*: 2020-08-26 |
Sponsor Name:Linkoping University | ||
Full Title: Effects of the FAAH inhibitor JNJ-42165279 in combination with internet-based cognitive behavioral therapy in PTSD | ||
Medical condition: post traumatic stress disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001279-18 | Sponsor Protocol Number: NHSCHECK | Start Date*: 2021-03-09 |
Sponsor Name:King’s College London | ||
Full Title: Overall Study Name: NHS CHECK - Health & Experiences of staff working at NHS Trusts and Nightingale Hospitals. Embedded RCT Full Title: Effectiveness of a smartphone app-based intervention in impr... | ||
Medical condition: Mental Health and Wellbeing of Healthcare Staff | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2021-000862-14 | Sponsor Protocol Number: A-bipolar | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:Copenhagen Affective Disorder research Center (CADIC), | |||||||||||||
Full Title: Effects of low dose Aspirin in bipolar disorder – a randomized controlled trial (the A-Bipolar RCT) | |||||||||||||
Medical condition: Bipolar disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011638-90 | Sponsor Protocol Number: 08082GM-A | Start Date*: 2009-11-09 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Targeting microvascular dysfunction in young hypertensive patients. | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-005013-47 | Sponsor Protocol Number: FAAH2 | Start Date*: 2017-02-28 | |||||||||||
Sponsor Name:Linköping University | |||||||||||||
Full Title: Effects of the FAAH inhibitor PF-04457845 on fear extinction in healthy volunteers | |||||||||||||
Medical condition: Healthy volunteers (extinction of fear) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005006-31 | Sponsor Protocol Number: EML053774_002 | Start Date*: 2007-04-03 |
Sponsor Name:Merck Sante France | ||
Full Title: A randomized, stratified on age, parallel group design study to investigate the safety, tolerability and pharmacokinetics after a 60 minutes application of 4% lidocaine cream compared to EMLA® crea... | ||
Medical condition: Topical anesthesia of healthy skin before venous or subcutaneous puncture, before superficial cutaneous instrumental surgery or laser beam (tattoo or cutaneousangioma) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005883-78 | Sponsor Protocol Number: CHRD1520 | Start Date*: 2021-02-05 | |||||||||||||||||||||||||||||||
Sponsor Name:Hospital Center rené Dubos | |||||||||||||||||||||||||||||||||
Full Title: Comparison of Prednisolone and Dexamethasone on D28 mortality in patients on oxygen therapy with CoViD-19 | |||||||||||||||||||||||||||||||||
Medical condition: Care of severe forms of CoViD-19 from the transitional phase and the onset of the inflammatory phase with corticosteroids | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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